366-53-0

Upstream product

• 1542-36-5 2,5-difluoro-4-nitroaniline 
• 367-30-6 2,5-difluoroaniline 
• 398-90-3 (2,5-difluorophenyl)acetanilide 

Downstream Products

• 344420-50-4 N-[2-fluoro-5-(2-hydroxyphenoxy)-4-nitrophenyl]acetamide 
• 104818-06-6 2-fluoro-4-nitro-5-(2-propynyl)aminoacetanilide 
• 1374780-52-5 N,N'-[2,5-bis(4-oxidomorpholin-4-yl)-1,4-phenylene]diacetamide 
• 133531-68-7 1,4-difluoro-2,5-dinitrobenzene 
• 1374780-41-2 4,4'-(2,5-dinitro-1,4-phenylene)dimorpholine 
• 1374780-43-4 1-[2,5-dinitro-4-(pyrrolidin-1-yl)phenyl]piperidine 
• 1374780-44-5 N,N'-[2,5-di(morpholin-4-yl)-1,4-phenylene]diacetamide 
• 1374780-46-7 N,N'-[2-(piperidin-1-yl)-5-(pyrrolidin-1-yl)-1,4-phenylene]diacetamide 
• 1542-36-5 2,5-difluoro-4-nitroaniline 
• 1454650-57-7 4-fluoro-2,5-dinitro-N-propylbenzeneamine 
• 1454650-59-9 4-fluoro-2,5-dinitro-N-propyl-N-trifluoroacetylbenzeneamine 
• 1454650-60-2 N-2,5-dinitro-4-butylaminophenyl-N-propyl-2,2,2-trifluoroacetamide 
• 1454650-61-3 2-butylamino-5-propylamino-1,4-dinitrobenzene 
• 1454650-56-6 1,4-diamino-2-butylamino-5-propylamino benzene 

Relevant academic research and scientific papers

COLLECTIONS OF PEPTIDES, PEPTIDE AGENTS, AND METHODS OF USE THEREOF

The present disclosure provides powerful technologies for the development, production, characterization, and/or use of stapled peptide compositions. Among other things, the present disclosure provides strategies for defining amino acid sequences particularly amenable or useful for stapling, as well as technologies, reagents, and systems for developing, producing, characterizing, and/or using stapled peptides having such amino acid sequences.

2,5-DISUBSTITUTED-1,4-DIAMINOBENZENES

Asymmetrical 2,5-disubstituted-1,4-diaminobenzenes are provided, along with a process for forming both symmetrical and asymmetrical 2,5-disubstituted-1,4-diaminobenzenes.

Synthesis and toxicity of new ring-fused imidazo[5,4-f] benzimidazolequinones and mechanism using amine N-oxide cyclizations

A new synthetic route to ring-fused imidazo[5,4-f]benzimidazoles is reported that can be used to access symmetrical and unsymmetrical quinone anticancer agents. Oxone in formic acid allows cyclisation of o-tert-aminoacetanilides to give ring-fused benzimi

6-heterocyclyl-1-(substituted phenyl)benzotriazole herbicidal agents

There is provided a 6-heterocyclyl-1-(substituted phenyl)benzotriazole compound having the structural formula I STR1 Further provided are a composition and a method comprising that compound for the control of undesirable plant species.

Herbicidal substituted-phenyl-1,2,4-triazol-5(1H)-thiones and -ones

The present application discloses herbicidal substituted-phenyl-1,2,4-Triazole-5(1H)-thiones and -ones, herbicidal compositions containing these compounds, methods of preparing them, and methods for controlling undesired plant growth by preemrgence and/or

Condensed heterocyclic derivatives and herbicides

A condensed heterocyclic derivative having the formula: STR1 wherein X is an oxygen atom or a sulfur atom; and Z is STR2